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Peroxisomal D-bifunctional protein deficiency: First case reports from Slovakia.
Konkoľová J, Petrovič R, Chandoga J, Repiský M, Zelinková H, Kršiaková J, Kolníková M, Kantarská D, Šutovský S, Böhmer D. Konkoľová J, et al. Among authors: kantarska d. Gene. 2015 Aug 15;568(1):61-8. doi: 10.1016/j.gene.2015.05.020. Epub 2015 May 9. Gene. 2015. PMID: 25967389
Influence of different spectra of NOTCH3 variants on the clinical phenotype of CADASIL - experience from Slovakia.
Juhosová M, Chandoga J, Cisárik F, Dallemule S, Ďurina P, Jarásková D, Jungová P, Kantarská D, Kvasnicová M, Mistrík M, Pastoráková A, Petrovič R, Valachová A, Zelinková H, Barošová J, Böhmer D, Štofko J. Juhosová M, et al. Among authors: kantarska d. Neurogenetics. 2023 Jan;24(1):1-16. doi: 10.1007/s10048-022-00704-6. Epub 2022 Nov 19. Neurogenetics. 2023. PMID: 36401683